chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97188307871883079AG14GENIChomozygous117719413
97188492371884924GA17GENIChomozygous117739292
97188577971885780AG25GENIChomozygous117719419
97188693471886935AG32GENIChomozygous117719421
97188702471887025TG32GENIChomozygous117719423
97188755771887558TC30GENIChomozygous117719427
97188804471888045TG22GENIChomozygous117719429
97188974471889745CT13GENIChomozygous117719435
97189185871891859GA21GENIChomozygous117719437
97189261971892620GT16GENIChomozygous117739320
97189292171892922AG23GENIChomozygous117719443
97189358571893586AG22GENIChomozygous117719445
97189615071896151AC15GENIChomozygous117719449
97189864671898647AG18GENIChomozygous117719455
97190119571901196GA27GENIChomozygous117739330
97190135071901351TA22GENIChomozygous117719459
97190285471902855AG16GENIChomozygous117719461
97190289971902900GA21GENIChomozygous117739336
97190580771905808TC27GENIChomozygous117719465
97190597571905976GA27GENIChomozygous117739340
97190660071906601TC27GENIChomozygous117719467
97190719571907196GA27GENIChomozygous117739346
97190797271907973GA33GENIChomozygous117739356
97190823971908240TC20GENIChomozygous117719473
97190850071908501GA23GENIChomozygous117719475
97190853071908531TC24GENIChomozygous117719477
97190856971908570AG22GENIChomozygous117719479
97190867971908680AT18GENIChomozygous117719481
97190919271909193TC14GENIChomozygous117739368
97190963271909633CT21GENIChomozygous117739370
97191035071910351TC16GENIChomozygous117719489
97191035171910352TG16GENIChomozygous117719491
97191041171910412TC14GENIChomozygous117719493
97191066071910661GA29GENIChomozygous117719495
97191116171911162TA25GENIChomozygous117719499
97191131271911313GC21GENIChomozygous117719501